Canonical Allele Identifier: CA272358

Gene: PAFAH1B1

Linked Data

• ClinVar Variation Id: 159489
• ClinVar RCV Id: RCV000147005
• dbSNP Id: rs587784236
• MyVariant Identifiers: chr17:g.2583464C>T (hg19) ; chr17:g.2680170C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2680170C>T , CM000679.2:g.2680170C>T	GRCh38
NC_000017.10:g.2583464C>T , CM000679.1:g.2583464C>T	GRCh37
NC_000017.9:g.2530214C>T	NCBI36
NG_009799.1:g.91542C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000397195.10:c.1009C>T MANE Select	ENSP00000380378.4:p.His337Tyr
ENST00000571495.2:n.2094C>T
ENST00000610190.2:n.561C>T
ENST00000674608.1:c.1063C>T	ENSP00000501976.1:p.His355Tyr
ENST00000674717.1:c.814C>T	ENSP00000501931.1:p.His272Tyr
ENST00000675084.1:n.263C>T
ENST00000675202.1:c.1009C>T	ENSP00000502843.1:p.His337Tyr
ENST00000675331.1:c.1009C>T	ENSP00000502031.1:p.His337Tyr
ENST00000675385.1:n.623C>T
ENST00000675390.1:c.1009C>T	ENSP00000501969.1:p.His337Tyr
ENST00000675574.1:n.4064C>T
ENST00000675621.1:c.*86-1559C>T	ENSP00000502117.1:n.*86-1559C>T
ENST00000675764.1:c.*963C>T	ENSP00000502242.1:n.*963C>T
ENST00000676077.1:c.*327C>T	ENSP00000502507.1:n.*327C>T
ENST00000676098.1:c.1009C>T	ENSP00000502735.1:p.His337Tyr
ENST00000676188.1:c.1009C>T	ENSP00000502577.1:p.His337Tyr
ENST00000676353.1:c.814C>T	ENSP00000502737.1:p.His272Tyr
ENST00000397193.7:n.817C>T
ENST00000397195.9:c.1009C>T	ENSP00000380378.4:p.His337Tyr
ENST00000571495.1:n.733C>T
ENST00000572915.6:n.677-3418C>T
ENST00000574468.1:c.403C>T	ENSP00000460591.1:p.His135Tyr
ENST00000574816.5:n.330C>T
ENST00000610190.1:n.484C>T
NM_000430.3:c.1009C>T	NP_000421.1:p.His337Tyr
XM_011523901.1:c.1063C>T	XP_011522203.1:p.His355Tyr
XM_011523902.1:c.1063C>T	XP_011522204.1:p.His355Tyr
XM_011523903.1:c.1063C>T	XP_011522205.1:p.His355Tyr
XM_011523901.2:c.1063C>T	XP_011522203.1:p.His355Tyr
XM_011523902.3:c.1063C>T	XP_011522204.1:p.His355Tyr
XM_011523903.2:c.1063C>T	XP_011522205.1:p.His355Tyr
XM_017024701.1:c.1009C>T	XP_016880190.1:p.His337Tyr
XM_017024702.2:c.814C>T	XP_016880191.1:p.His272Tyr
NM_000430.4:c.1009C>T MANE Select	NP_000421.1:p.His337Tyr